4.6 Review

Regulatory T cell identity: formation and maintenance

期刊

TRENDS IN IMMUNOLOGY
卷 36, 期 6, 页码 344-353

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.it.2015.04.006

关键词

regulatory T cell; Foxp3; TCR; DNA looping; CpG methylation

资金

  1. Nomis Foundation
  2. Rita Allen Foundation
  3. Hearst Foundation
  4. National Multiple Sclerosis Society
  5. National Institute of Health [AI099295, AI107027]

向作者/读者索取更多资源

T regulatory (Treg) cells are central to the maintenance of immune homeostasis. The transcription factor forkhead box P3 (Foxp3) is essential for specifying the Treg cell lineage during development, and continued expression of Foxp3 in mature Treg cells is necessary for suppressive function. Loss of Foxp3 expression in Treg cells is associated with autoimmune pathology. Here, we review recent insights into the mechanisms that maintain Treg cell stability and function, and place these findings within the broader understanding of mechanisms that establish Treg cell identity during development. We integrate emerging principles in Treg cell lineage maintenance with the mechanisms that allow Treg cells to sense and respond to varied inflammatory environments, and outline important areas of future inquiry in this context.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据